Cited by 784Neuroscience and Neuropharmacology ResearchVisual perception and processing mechanismsNeurogenesis and neuroplasticity mechanisms

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Patterned Activity, Synaptic Convergence, and the NMDA Receptor in Developing Visual Pathways

Constantine-Paton, M, Cline, H T, Debski, E·1990·Annual Review of Neuroscience

DOI 10.1146/annurev.ne.13.030190.001021

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The brain's default mode network consists of discrete, bilateral and symmetrical cortical areas, in the medial and lateral parietal, medial prefrontal, and medial and lateral temporal cortices of the human, nonhuman primate, cat, and rodent brains. Its ...Read More

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Magnesium gates glutamate-activated channels in mouse central neurones
Nowak, L. M., Bregestovski, P. D., Ascher, P., Herbet, A., & Prochiantz, A. (1984) · Nature · doi:10.1038/307462a0 · Cited by 4,116
Voltage-dependent block by Mg2+ of NMDA responses in spinal cord neurones
Mayer, M. L., Westbrook, G. L., & Guthrie, P. B. (1984) · Nature · doi:10.1038/309261a0 · Cited by 2,941
SINGLE-CELL RESPONSES IN STRIATE CORTEX OF KITTENS DEPRIVED OF VISION IN ONE EYE
Wiesel, T. N., & Hubel, D. H. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.1003 · Cited by 2,628
Plasticity of ocular dominance columns in monkey striate cortex
Hubel, D. H., Wiesel, T. N., LeVay, S., Barlow, H. B., & Gaze, R. M. (1977) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1977.0050 · Cited by 1,629
Selective stabilisation of developing synapses as a mechanism for the specification of neuronal networks
Changeux, J.-P., & Danchin, A. (1976) · Nature · doi:10.1038/264705a0 · Cited by 1,448
BINOCULAR INTERACTION IN STRIATE CORTEX OF KITTENS REARED WITH ARTIFICIAL SQUINT
Hubel, D. H., & Wiesel, T. N. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.6.1041 · Cited by 1,369
The development of ocular dominance columns in normal and visually deprived monkeys
Le Vay, S., Wiesel, T. N., & Hubel, D. H. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901910102 · Cited by 1,123
Organization of Behavior.
Kaplan, S. J. (1950) · PubMed Central · Cited by 1,050
The Biochemistry of Memory: A New and Specific Hypothesis
LYNCH, G. S., & Baudry, M. (1984) · Science · doi:10.1126/science.6144182 · Cited by 1,041
Long-term potentiation and NMDA receptors in rat visual cortex
Artola, A., & Singer, W. (1987) · Nature · doi:10.1038/330649a0 · Cited by 967
Blockade of "NMDA" Receptors Disrupts Experience-Dependent Plasticity of Kitten Striate Cortex
Kleinschmidt, A. K., Bear, M. F., & Singer, W. (1987) · Science · doi:10.1126/science.2443978 · Cited by 911
Modulation of visual cortical plasticity by acetylcholine and noradrenaline
Bear, M. F., & Singer, W. (1986) · Nature · doi:10.1038/320172a0 · Cited by 858
Long-Term Potentiation
Teyler, T. J., & DiScenna, P. G. (1987) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.10.030187.001023 · Cited by 815
Organization of visual pathways in normal and visually deprived cats.
Sherman, S. M., & Spear, P. D. (1982) · Physiological Reviews · doi:10.1152/physrev.1982.62.2.738 · Cited by 704
Ocular dominance in layer IV of the cat's visual cortex and the effects of monocular deprivation.
Shatz, C. J., & Stryker, M. P. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012421 · Cited by 691
Binocular impulse blockade prevents the formation of ocular dominance columns in cat visual cortex
Stryker, M., & Harris, W. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-08-02117.1986 · Cited by 687
Visual Experience Modifies Distribution of Horizontally and Vertically Oriented Receptive Fields in Cats
Hirsch, H. V. B., & Spinelli, D. N. (1970) · Science · doi:10.1126/science.168.3933.869 · Cited by 588
The current excitement in long term potentiation
Nicoll, R. A., Kauer, J. A., & Malenka, R. C. (1988) · Neuron · doi:10.1016/0896-6273(88)90193-6 · Cited by 535
A Physiological Basis for a Theory of Synapse Modification
Bear, M. F., Cooper, L. N., & Ebner, F. F. (1987) · Science · doi:10.1126/science.3037696 · Cited by 528
Motor Nerve Sprouting
Brown, M. C., Holland, R. L., & Hopkins, W. G. (1981) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.04.030181.000313 · Cited by 528
N-methyl-D-aspartate receptor antagonist desegregates eye-specific stripes.
Cline, H. T., Debski, E. A., & Constantine‐Paton, M. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.12.4342 · Cited by 525
Self-citation
Reversal of the physiological effects of monocular deprivation in kittens: further evidence for a sensitive period
Blakemore, C. B., & Sluyters, R. C. V. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010478 · Cited by 452
Microcircuitry of the Visual Cortex
Gilbert, C. D. (1983) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.06.030183.001245 · Cited by 451
NMDA receptors in the visual cortex of young kittens are more effective than those of adult cats
Tsumoto, T., Hagihara, K., Sato, H., & Hata, Y. (1987) · Nature · doi:10.1038/327513a0 · Cited by 440
Visual Neural Development
Movshon, J. A., & Sluyters, R. C. V. (1981) · Annual Review of Psychology · doi:10.1146/annurev.ps.32.020181.002401 · Cited by 408
The role of NMDA receptors in learning and memory
Collingridge, G. L. (1987) · Nature · doi:10.1038/330604a0 · Cited by 373
Binocular competition in the control of geniculate cell growth
Guillery, R. W. (1972) · The Journal of Comparative Neurology · doi:10.1002/cne.901440106 · Cited by 337
Formation Of Topographic Maps
Udin, S. B., & Fawcett, J. W. (1988) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.11.030188.001445 · Cited by 309
The differential effects of unilateral lid closure upon the monocular and binocular segments of the dorsal lateral geniculate nucleus in the cat
Guillery, R. W., & Stelzner, D. J. (1970) · The Journal of Comparative Neurology · doi:10.1002/cne.901390403 · Cited by 307
The location and function of NMDA receptors in cat and kitten visual cortex
Fox, K., Sato, H., & Daw, N. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-07-02443.1989 · Cited by 307
NMDA receptor antagonists disrupt the retinotectal topographic map
Cline, H. T., & Constantine‐Paton, M. (1989) · Neuron · doi:10.1016/0896-6273(89)90201-8 · Cited by 285
Self-citation
Suppression of Neurite Elongation and Growth Cone Motility by Electrical Activity
Cohan, C. S., & Kater, S. B. (1986) · Science · doi:10.1126/science.3715470 · Cited by 278
Pharmacological Induction of Use-Dependent Receptive Field Modifications in the Visual Cortex
Greuel, J. M., Luhmann, H. J., & Singer, W. (1988) · Science · doi:10.1126/science.2902687 · Cited by 276
Long-term potentiation in the dentate gyrus: induction and increased glutamate release are blocked by d(−)aminophosphonovalerate
Errington, M. L., Lynch, M. A., & Bliss, T. V. P. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90019-4 · Cited by 274
Neural plasticity without postsynaptic action potentials: less-active inputs become dominant when kitten visual cortical cells are pharmacologically inhibited.
Reiter, H. O., & Stryker, M. P. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.10.3623 · Cited by 266
Eye-Specific Termination Bands in Tecta of Three-Eyed Frogs
Constantine‐Paton, M., & Law, M. I. (1978) · Science · doi:10.1126/science.309179 · Cited by 264
Self-citation
Correlated firing of cat retinal ganglion cells. I. Spontaneously active inputs to X- and Y-cells
Mastronarde, D. N. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.2.303 · Cited by 258
Activity sharpens the map during the regeneration of the retinotectal projection in goldfish
Schmidt, J. T., & Edwards, D. L. (1983) · Brain Research · doi:10.1016/0006-8993(83)90959-9 · Cited by 247
The physiological effects of monocular deprivation and their reversal in the monkey's visual cortex.
Blakemore, C. B., Garey, L. J., & Vital‐Durand, F. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012498 · Cited by 233
The effects of early visual experience on the cat's visual cortex and their possible explanation by Hebb synapses.
Rauschecker, J. P., & Singer, W. (1981) · The Journal of Physiology · doi:10.1113/jphysiol.1981.sp013545 · Cited by 220
Changes in the postsynaptic density with long‐term potentiation in the dentate gyrus
Desmond, N. L., & Levy, W. B. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902530405 · Cited by 207
Ketamine—xylazine anaesthesia blocks consolidation of ocular dominance changes in kitten visual cortex
Rauschecker, J. P., & Hahn, S. (1987) · Nature · doi:10.1038/326183a0 · Cited by 202
Tetrodotoxin Blocks the Formation of Ocular Dominance Columns in Goldfish
Meyer, R. L. (1982) · Science · doi:10.1126/science.7123262 · Cited by 186
Tetrodotoxin inhibits the formation of refined retinotopography in goldfish
Meyer, R. L. (1983) · Developmental Brain Research · doi:10.1016/0165-3806(83)90068-8 · Cited by 186
Central gating of developmental plasticity in kitten visual cortex
Singer, W., Tretter, F., & Yinon, U. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014108 · Cited by 184
A role for action-potential activity in the development of neuronal connections in the kitten retinogeniculate pathway
Dubin, M. W., Stark, L. A., & Archer, S. M. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-04-01021.1986 · Cited by 179
Postcritical-period reversal of effects of monocular deprivation on striate cortex cells in the cat
Kratz, K. E., & Spear, P. D. (1976) · Journal of Neurophysiology · doi:10.1152/jn.1976.39.3.501 · Cited by 169
An evaluation of the hypothesis of shifting terminals in goldfish optic tectum
Easter, S., & Stuermer, C. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-04-01052.1984 · Cited by 166
Interactions between ganglion cells in cat retina
Mastronarde, D. N. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.2.350 · Cited by 163
On long‐lasting potentiation in the hippocampus. a proposed mechanism for its dependence on coincident pre‐ and postsynaptic activity
Wigström, H., & Gustafsson, B. (1985) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1985.tb07621.x · Cited by 134
The function of dendritic spines: A review of theoretical issues
Coss, R. G., & Perkel, D. H. (1985) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(85)90170-0 · Cited by 134
Abnormal Development of Kitten Retino-Geniculate Connectivity in the Absence of Action Potentials
Archer, S. M., Dubin, M. W., & Stark, L. A. (1982) · Science · doi:10.1126/science.7100921 · Cited by 122
Statistical dependence between neighboring retinal ganglion cells in goldfish
Arnett, D. W. (1978) · Experimental Brain Research · doi:10.1007/bf00237389 · Cited by 122
A critical period for long-term potentiation in the developing rat visual cortex
Perkins, A. T., & Teyler, T. J. (1988) · Brain Research · doi:10.1016/0006-8993(88)91478-3 · Cited by 117
Cortical activity blockade prevents ocular dominance plasticity in the kitten visual cortex
Reiter, H. O., Waitzman, D. M., & Stryker, M. P. (1986) · Experimental Brain Research · doi:10.1007/bf00243841 · Cited by 108
Cross‐correlation analysis of the maintained discharge of rabbit retinal ganglion cells.
Arnett, D., & Spraker, T. E. (1981) · The Journal of Physiology · doi:10.1113/jphysiol.1981.sp013812 · Cited by 97
Anatomy and physiology of experimentally produced striped tecta
Law, M. I., & Constantine‐Paton, M. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-07-00741.1981 · Cited by 92
Self-citation
Ocular dominance shift in kitten visual cortex caused by imbalance in retinal electrical activity
Chapman, B., Jacobson, M. D., Reiter, H. O., & Stryker, M. P. (1986) · Nature · doi:10.1038/324154a0 · Cited by 89
Discontinuous mapping of retina onto tectum innervated by both eyes
Levine, R. L., & Jacobson, M. (1975) · Brain Research · doi:10.1016/0006-8993(75)90517-x · Cited by 88
Central core control of developmental plasticity in the kitten visual cortex: II. Electrical activation of mesencephalic and diencephalic projections
Singer, W., & Rauschecker, J. P. (1982) · Experimental Brain Research · doi:10.1007/bf00239381 · Cited by 88
Activity and the formation of ocular dominance patches in dually innervated tectum of goldfish
Boss, V., & Schmidt, J. T. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-12-02891.1984 · Cited by 84
Effects of 6-hydroxydopamine on visual deprivation in the kitten striate cortex
Daw, N. W., Rader, R. K., Robertson, T., & Ariel, M. (1983) · Journal of Neuroscience · doi:10.1523/jneurosci.03-05-00907.1983 · Cited by 81
Disruption of cortical activity prevents ocular dominance changes in monocularly deprived kittens
Shaw, C., & Cynader, M. (1984) · Nature · doi:10.1038/308731a0 · Cited by 74
Actions of excitatory amino acid antagonists on geniculo-cortical transmission in the cat's visual cortex
Hagihara, K., Tsumoto, T., Sato, H., & Hata, Y. (1988) · Experimental Brain Research · doi:10.1007/bf00247586 · Cited by 71
Evidence for shifting connections during development of the chick retinotectal projection
McLoon, S. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-10-02570.1985 · Cited by 65
Pharmacology of retinotectal transmission in the goldfish: effects of nicotinic ligands, strychnine, and kynurenic acid
Langdon, R., & Freeman, J. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-03-00760.1987 · Cited by 61
DSP-4 (N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine) depletes noradrenaline in kitten visual cortex without altering the effects of monocular deprivation
Daw, N. W., Videen, T., Parkinson, D., & Rader, R. K. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-07-01925.1985 · Cited by 59
Abnormal visual input leads to development of abnormal axon trajectories in frogs
Udin, S. B. (1983) · Nature · doi:10.1038/301336a0 · Cited by 58
Role of visual experience in promoting segregation of eye dominance patches in the visual cortex of the cat
Swindale, N. V. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902670403 · Cited by 55
Visual deprivation and intertectal neuronal connexions in Xenopus laevis
Keating, M. J., & Feldman, J. D. (1975) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1975.0139 · Cited by 49
Compound eyes project stripes on the optic tectum in Xenopus
Fawcett, J. W., & Willshaw, D. J. (1982) · Nature · doi:10.1038/296350a0 · Cited by 47
Eye Dominance Columns from an Isogenic Double-Nasal Frog Eye
Ide, C. F., Fraser, S. E., & Meyer, R. L. (1983) · Science · doi:10.1126/science.6857287 · Cited by 40
Intraocular injection of tetrodotoxin in goldfish decreases fast axonal transport of [3H]glucosamine-labeled materials in optic axons
Edwards, D. L., & Grafstein, B. (1984) · Brain Research · doi:10.1016/0006-8993(84)90807-2 · Cited by 35
Development and Plasticity of Retinal X and Y Axon Terminations in the Cat's Lateral Geniculate Nucleus
Sur, M. (2008) · Brain Behavior and Evolution · doi:10.1159/000116592 · Cited by 30
Long-term potentiation in the goldfish optic tectum
LEWIS, D. A., & Teyler, T. J. (1986) · Brain Research · doi:10.1016/0006-8993(86)90744-4 · Cited by 24
Specificity of regenerating optic fibres for left and right optic tecta in goldfish
Cronly-Dillon, J. R., & Glaizner, B. (1974) · Nature · doi:10.1038/251505b0 · Cited by 18
Increased potentiation of postsynaptic responses correlates with sensitive period during optic nerve regeneration in goldfish
Schmidt, J. T. (1987) · The Society for Neuroscience Abstracts · Cited by 4

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Authors: Constantine-Paton, M., Cline, H. T., & Debski, E.
ORCID: Cline, H T
Venue: Annual Review of Neuroscience
Publisher: Annual Reviews
Published: 1990-03
Volume: 13
Issue: 1
Pages: 129-154
ISSN: 0147-006X (ISSN-L)
1545-4126
DOI: 10.1146/annurev.ne.13.030190.001021
OpenAlex: W1986240433
Cited by: 784
References: 77
Citations by year: 2025: 3 · 2024: 2 · 2023: 22 · 2022: 3 · 2021: 4 · 2020: 6 · 2019: 7 · 2018: 2 · 2017: 5 · 2016: 9 · 2015: 10 · 2014: 7 · 2013: 11 · 2012: 13
FWCI: 16.15
Type: journal article
Language: en
Open access: closed
Locations: Annual Review of Neuroscience (publishedVersion)
PubMed (publishedVersion)
Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords: NMDA receptor, synaptic convergence, visual pathway development, default mode network, visual cortex development
MeSH terms: Animals, Geniculate Bodies, Functional Laterality, Neuronal Plasticity, Retina, Visual Cortex, Visual Pathways

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Patterned Activity, Synaptic Convergence, and the NMDA Receptor in Developing Visual Pathways

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